作者: Cheng-Yu Wang , Linxi Wang , Andrew Belnick , Hao Wang , Jing Li
DOI: 10.1016/J.CES.2017.02.020
关键词: Selectivity 、 Adsorption 、 Nitrogen 、 Air separation 、 Pressure swing adsorption 、 Oxygen 、 Carbon dioxide 、 Inorganic chemistry 、 Chemistry 、 Selective adsorption
摘要: Abstract Development of an oxygen selective adsorbent is anticipated to reduce the material and energy requirements for adsorptive separations air by a factor four, due relative concentrations N 2 O in air, thereby decreasing parasitic losses, carbon dioxide emissions, cost purification via pressure-swing adsorption. Here, we report that RPM3-Zn (a.k.a. Zn (bpdc) (bpee); bpdc = 4,4′-biphenyldicarboxylate; bpee = 1,2-bipyridylethene) over nitrogen at temperatures from 77 K 273 K, although capacity sorbent decreased markedly increasing temperatures. Due diffusivity ∼1000-fold greater than nitrogen, effective selectivity increases near infinity low temperature equal contact times mass transfer limitations gate-opening. The kinetic limitation open structure has sharp dependence, suggesting this may be “tuned in” other flexible metal-organic-frameworks. Although not practical displace cryogenic distillation, results suggest new mechanism tailoring materials selectivity, namely, capitalizing upon delayed opening process particular gas another.